Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 284996 |
| ensemblid | ENSG00000163162.9 |
| hgncid | 23137 |
| symbol | RNF149 |
| name | ring finger protein 149 |
| refseq_nuc | NM_173647.4 |
| refseq_prot | NP_775918.2 |
| ensembl_nuc | ENST00000295317.4 |
| ensembl_prot | ENSP00000295317.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 101275601 |
| end | 101308701 |
| strand | - |
| ver | v1.2 |
| region | chr2:101275601-101308701 |
| region5000 | chr2:101270601-101313701 |
| regionname0 | RNF149_chr2_101275601_101308701 |
| regionname5000 | RNF149_chr2_101270601_101313701 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 400 | 181 | 18 | 31 | 94 | 13 | 25 | 74 | RNF149_chr2_101270601_101313701 | RNF149 | MAWRR others(395): Show |
chr2 | 101270601 | 101313701 |
| a0002 | 0/0 | 400 | 139 | 39 | 23 | 63 | 2 | 12 | 54 | RNF149_chr2_101270601_101313701 | RNF149 | MAWRR others(395): Show |
chr2 | 101270601 | 101313701 |
| a0003 | 0/1 | 400 | 46 | 30 | 8 | 0 | 1 | 6 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | MAWRR others(395): Show |
chr2 | 101270601 | 101313701 |
| a0004 | 0/0 | 400 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | MAWRR others(395): Show |
chr2 | 101270601 | 101313701 |
| a0005 | 0/0 | 400 | 3 | 0 | 2 | 1 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | MAWRR others(395): Show |
chr2 | 101270601 | 101313701 |
| a0006 | 1/0 | 400 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | MAWRR others(395): Show |
chr2 | 101270601 | 101313701 |
| a0007 | 0/0 | 400 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | MAWRR others(395): Show |
chr2 | 101270601 | 101313701 |
| a0008 | 0/0 | 400 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | MAWRR others(395): Show |
chr2 | 101270601 | 101313701 |
| a0009 | 0/0 | 400 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | MAWRR others(395): Show |
chr2 | 101270601 | 101313701 |
| a0010 | 0/0 | 400 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | MAWRR others(395): Show |
chr2 | 101270601 | 101313701 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1200 | 181 | 18 | 31 | 94 | 13 | 25 | RNF149_chr2_101270601_101313701 | RNF149 | ATGGC others(1195): Show |
chr2 | 101270601 | 101313701 | ||
| a0002c0002 | 0/0 | 1200 | 139 | 39 | 23 | 63 | 2 | 12 | RNF149_chr2_101270601_101313701 | RNF149 | ATGGC others(1195): Show |
chr2 | 101270601 | 101313701 | ||
| a0003c0003 | 0/1 | 1200 | 46 | 30 | 8 | 0 | 1 | 6 | RNF149_chr2_101270601_101313701 | RNF149 | ATGGC others(1195): Show |
chr2 | 101270601 | 101313701 | ||
| a0004c0004 | 0/0 | 1200 | 4 | 4 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | ATGGC others(1195): Show |
chr2 | 101270601 | 101313701 | ||
| a0005c0005 | 0/0 | 1200 | 3 | 0 | 2 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | ATGGC others(1195): Show |
chr2 | 101270601 | 101313701 | ||
| a0006c0006 | 1/0 | 1200 | 1 | 0 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | ATGGC others(1195): Show |
chr2 | 101270601 | 101313701 | ||
| a0007c0008 | 0/0 | 1200 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | ATGGC others(1195): Show |
chr2 | 101270601 | 101313701 | ||
| a0008c0010 | 0/0 | 1200 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | ATGGC others(1195): Show |
chr2 | 101270601 | 101313701 | ||
| a0009c0007 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | ATGGC others(1195): Show |
chr2 | 101270601 | 101313701 | ||
| a0010c0009 | 0/0 | 1200 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | ATGGC others(1195): Show |
chr2 | 101270601 | 101313701 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2953 | 176 | 18 | 31 | 94 | 10 | 23 | RNF149_chr2_101270601_101313701 | RNF149 | GACCC others(2948): Show |
chr2 | 101270601 | 101313701 |
| a0001c0001t0003 | 0/0 | 2953 | 3 | 0 | 0 | 0 | 3 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | GACCC others(2948): Show |
chr2 | 101270601 | 101313701 |
| a0001c0001t0006 | 0/0 | 2953 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | GACCC others(2948): Show |
chr2 | 101270601 | 101313701 |
| a0001c0001t0007 | 0/0 | 2953 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | GACCC others(2948): Show |
chr2 | 101270601 | 101313701 |
| a0002c0002t0001 | 0/0 | 2953 | 135 | 36 | 23 | 63 | 2 | 11 | RNF149_chr2_101270601_101313701 | RNF149 | GACCC others(2948): Show |
chr2 | 101270601 | 101313701 |
| a0002c0002t0005 | 0/0 | 2953 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | GACCC others(2948): Show |
chr2 | 101270601 | 101313701 |
| a0002c0002t0009 | 0/0 | 2811 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | GACCC others(2806): Show |
chr2 | 101270601 | 101313701 |
| a0002c0002t0010 | 0/0 | 2953 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | GACCC others(2948): Show |
chr2 | 101270601 | 101313701 |
| a0002c0002t0011 | 0/0 | 2953 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | GACCC others(2948): Show |
chr2 | 101270601 | 101313701 |
| a0003c0003t0001 | 0/1 | 2953 | 41 | 25 | 8 | 0 | 1 | 6 | RNF149_chr2_101270601_101313701 | RNF149 | GACCC others(2948): Show |
chr2 | 101270601 | 101313701 |
| a0003c0003t0004 | 0/0 | 2953 | 3 | 3 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | GACCC others(2948): Show |
chr2 | 101270601 | 101313701 |
| a0003c0003t0008 | 0/0 | 2953 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | GACCC others(2948): Show |
chr2 | 101270601 | 101313701 |
| a0003c0003t0012 | 0/0 | 2953 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | GACCC others(2948): Show |
chr2 | 101270601 | 101313701 |
| a0004c0004t0002 | 0/0 | 2950 | 4 | 4 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | GACCC others(2945): Show |
chr2 | 101270601 | 101313701 |
| a0005c0005t0001 | 0/0 | 2953 | 3 | 0 | 2 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | GACCC others(2948): Show |
chr2 | 101270601 | 101313701 |
| a0006c0006t0001 | 1/0 | 2953 | 1 | 0 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | GACCC others(2948): Show |
chr2 | 101270601 | 101313701 |
| a0007c0008t0001 | 0/0 | 2953 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | GACCC others(2948): Show |
chr2 | 101270601 | 101313701 |
| a0008c0010t0001 | 0/0 | 2953 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | GACCC others(2948): Show |
chr2 | 101270601 | 101313701 |
| a0009c0007t0001 | 0/0 | 2953 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | GACCC others(2948): Show |
chr2 | 101270601 | 101313701 |
| a0010c0009t0001 | 0/0 | 2953 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | GACCC others(2948): Show |
chr2 | 101270601 | 101313701 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 27 | 3 | 6 | 15 | 1 | 2 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0004 | 0/0 | 9 | 0 | 5 | 4 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0017 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0019 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0003g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0006g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0001c0001t0007g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0002 | 0/0 | 22 | 2 | 4 | 11 | 2 | 3 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0003 | 0/0 | 14 | 4 | 0 | 10 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0005 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0013 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0026 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0048 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0005g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0009g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0010g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0002c0002t0011g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0023 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0040 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0003c0003t0012g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0004c0004t0002g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0005c0005t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0005c0005t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0005c0005t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0006c0006t0001g0117 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0007c0008t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0008c0010t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0009c0007t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| a0010c0009t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0032 | EUR | GBR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | GBR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | GBR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | FIN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | FIN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | FIN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | CHS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | CHS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00642 | hp2 | a0003 | c0003 | t0001 | g0023 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0165 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0044 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0181 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01074 | hp2 | a0003 | c0003 | t0001 | g0023 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0044 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01099 | hp2 | a0003 | c0003 | t0001 | g0177 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01167 | hp1 | a0005 | c0005 | t0001 | g0108 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01167 | hp2 | a0003 | c0003 | t0001 | g0167 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01169 | hp1 | a0005 | c0005 | t0001 | g0092 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01175 | hp2 | a0003 | c0003 | t0001 | g0157 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0048 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01255 | hp1 | a0003 | c0003 | t0001 | g0168 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0204 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01346 | hp2 | a0003 | c0003 | t0001 | g0176 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0214 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0202 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01361 | hp2 | a0003 | c0003 | t0001 | g0169 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0184 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0186 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0137 | EUR | IBS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0032 | EUR | IBS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0166 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0164 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0154 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02040 | hp1 | a0007 | c0008 | t0001 | g0144 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02145 | hp1 | a0003 | c0003 | t0001 | g0008 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02145 | hp2 | a0002 | c0002 | t0010 | g0152 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0156 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02258 | hp2 | a0004 | c0004 | t0002 | g0016 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0150 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0196 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02451 | hp2 | a0003 | c0003 | t0001 | g0151 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02572 | hp1 | a0003 | c0003 | t0001 | g0161 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0212 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02602 | hp1 | a0008 | c0010 | t0001 | g0220 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02615 | hp1 | a0009 | c0007 | t0001 | g0139 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02615 | hp2 | a0003 | c0003 | t0001 | g0170 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02622 | hp1 | a0003 | c0003 | t0001 | g0159 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02647 | hp2 | a0003 | c0003 | t0001 | g0008 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02683 | hp2 | a0003 | c0003 | t0001 | g0037 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02698 | hp2 | a0003 | c0003 | t0001 | g0049 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02717 | hp1 | a0003 | c0003 | t0001 | g0145 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02723 | hp1 | a0003 | c0003 | t0004 | g0180 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0038 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02809 | hp2 | a0003 | c0003 | t0001 | g0024 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0201 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02818 | hp2 | a0003 | c0003 | t0012 | g0221 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0008 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02895 | hp1 | a0003 | c0003 | t0001 | g0160 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02896 | hp1 | a0003 | c0003 | t0001 | g0024 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0024 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02965 | hp2 | a0003 | c0003 | t0008 | g0173 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0203 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03017 | hp1 | a0003 | c0003 | t0001 | g0215 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03017 | hp2 | a0003 | c0003 | t0001 | g0040 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03041 | hp1 | a0003 | c0003 | t0004 | g0179 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0185 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0042 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03130 | hp2 | a0004 | c0004 | t0002 | g0016 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03139 | hp2 | a0004 | c0004 | t0002 | g0016 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03209 | hp2 | a0003 | c0003 | t0001 | g0158 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03225 | hp2 | a0002 | c0002 | t0009 | g0217 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0193 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0026 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03453 | hp1 | a0003 | c0003 | t0001 | g0199 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03453 | hp2 | a0003 | c0003 | t0001 | g0175 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0218 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03516 | hp1 | a0002 | c0002 | t0011 | g0200 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03540 | hp1 | a0003 | c0003 | t0001 | g0171 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03579 | hp1 | a0003 | c0003 | t0001 | g0172 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0216 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0147 | SAS | STU | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | STU | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03704 | hp1 | a0001 | c0001 | t0007 | g0063 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0148 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03831 | hp2 | a0001 | c0001 | t0006 | g0123 | SAS | BEB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0187 | SAS | BEB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03942 | hp2 | a0003 | c0003 | t0001 | g0037 | SAS | BEB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | STU | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG04204 | hp1 | a0002 | c0002 | t0005 | g0191 | SAS | STU | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | STU | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0213 | SAS | STU | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0153 | AFR | YRI | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18906 | hp1 | a0003 | c0003 | t0001 | g0039 | AFR | YRI | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18906 | hp2 | a0003 | c0003 | t0001 | g0038 | AFR | YRI | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18970 | hp1 | a0005 | c0005 | t0001 | g0094 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0194 | AFR | LWK | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19030 | hp2 | a0003 | c0003 | t0001 | g0040 | AFR | LWK | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19043 | hp1 | a0003 | c0003 | t0004 | g0146 | AFR | LWK | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19043 | hp2 | a0004 | c0004 | t0002 | g0016 | AFR | LWK | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19077 | hp1 | a0010 | c0009 | t0001 | g0219 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0206 | AFR | YRI | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ASW | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | TSI | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | TSI | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA20805 | hp2 | a0003 | c0003 | t0001 | g0023 | EUR | TSI | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA20905 | hp1 | a0003 | c0003 | t0001 | g0049 | SAS | GIH | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0192 | SAS | GIH | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | CLM | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0149 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0183 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02559 | hp1 | a0003 | c0003 | t0001 | g0174 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0042 | AFR | ACB | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0048 | AFR | MSL | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | USA | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| HG06807 | hp2 | a0003 | c0003 | t0001 | g0008 | AFR | USA | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | USA | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA20300 | hp2 | a0003 | c0003 | t0001 | g0039 | AFR | USA | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA21309 | hp1 | a0003 | c0003 | t0001 | g0008 | AFR | LWK | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | LWK | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0001 | g0155 | REF | REF | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| homoSapiens | grch38p0 | a0006 | c0006 | t0001 | g0117 | REF | REF | RNF149_chr2_101270601_101313701 | RNF149 | chr2 | 101270601 | 101313701 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:101281950 | G | C | 7 | a0001 a0002 a0005 others(4): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
missense_variant | MODERATE | c.1068C>G | p.Asp356Glu | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/7 | 1181/2953 | 1068/1203 | 356/400 | chr2 | 101281950 | |||
| chr2:101295026 | T | C | 1 | a0005 | 3 | HG01167.hp1 HG01169.hp1 NA18970.hp1 |
missense_variant | MODERATE | c.616A>G | p.Ile206Val | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/7 | 729/2953 | 616/1203 | 206/400 | chr2 | 101295026 | |||
| chr2:101295168 | T | C | 1 | a0009 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.474A>G | p.Ile158Met | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/7 | 587/2953 | 474/1203 | 158/400 | chr2 | 101295168 | |||
| chr2:101308261 | C | A | 1 | a0010 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.328G>T | p.Val110Phe | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/7 | 441/2953 | 328/1203 | 110/400 | chr2 | 101308261 | |||
| chr2:101308546 | C | T | 1 | a0007 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.43G>A | p.Val15Met | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/7 | 156/2953 | 43/1203 | 15/400 | chr2 | 101308546 | |||
| chr2:101308552 | G | A | 1 | a0004 | 4 | HG02258.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
missense_variant | MODERATE | c.37C>T | p.Arg13Cys | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/7 | 150/2953 | 37/1203 | 13/400 | chr2 | 101308552 | |||
| chr2:101308564 | T | C | 6 | a0002 a0003 a0004 others(3): Show |
191 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(188): Show |
missense_variant | MODERATE | c.25A>G | p.Ser9Gly | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/7 | 138/2953 | 25/1203 | 9/400 | chr2 | 101308564 | |||
| chr2:101308573 | G | A | 1 | a0008 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.16C>T | p.Arg6Cys | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/7 | 129/2953 | 16/1203 | 6/400 | chr2 | 101308573 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:101275643 | G | A | 9 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(6): Show |
169 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*1595C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 1595 | chr2 | 101275643 | ||||||
| chr2:101275651 | C | T | 4 | a0003c0003t0004 a0003c0003t0008 a0003c0003t0012 others(1): Show |
9 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1587G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 1587 | chr2 | 101275651 | ||||||
| chr2:101275652 | G | A | 1 | a0001c0001t0001 | 2 | HG00621.hp2 HG02071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1586C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 1586 | chr2 | 101275652 | ||||||
| chr2:101275670 | T | C | 1 | a0002c0002t0001 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1568A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 1568 | chr2 | 101275670 | ||||||
| chr2:101275676 | C | T | 5 | a0001c0001t0001 a0001c0001t0007 a0002c0002t0001 others(2): Show |
136 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*1562G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 1562 | chr2 | 101275676 | ||||||
| chr2:101275677 | G | A | 1 | a0002c0002t0001 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1561C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 1561 | chr2 | 101275677 | ||||||
| chr2:101275973 | T | C | 4 | a0003c0003t0004 a0003c0003t0008 a0003c0003t0012 others(1): Show |
9 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1265A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 1265 | chr2 | 101275973 | ||||||
| chr2:101276033 | A | G | 1 | a0002c0002t0009 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1205T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 1205 | chr2 | 101276033 | ||||||
| chr2:101276172 | C | T | 1 | a0001c0001t0007 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1066G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 1066 | chr2 | 101276172 | ||||||
| chr2:101276544 | T | C | 1 | a0002c0002t0009 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*694A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 694 | chr2 | 101276544 | ||||||
| chr2:101276573 | AAAT | A | 1 | a0004c0004t0002 | 4 | HG02258.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*662_*664delATT | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 662 | chr2 | 101276573 | ||||||
| chr2:101276778 | A | T | 3 | a0003c0003t0004 a0003c0003t0012 a0004c0004t0002 |
8 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*460T>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 460 | chr2 | 101276778 | ||||||
| chr2:101276895 | A | T | 1 | a0001c0001t0006 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*343T>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 343 | chr2 | 101276895 | ||||||
| chr2:101277064 | A | G | 1 | a0001c0001t0003 | 3 | HG00099.hp1 HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*174T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 174 | chr2 | 101277064 | ||||||
| chr2:101277120 | T | C | 1 | a0002c0002t0010 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*118A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 118 | chr2 | 101277120 | ||||||
| chr2:101277187 | C | G | 1 | a0002c0002t0005 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*51G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 51 | chr2 | 101277187 | ||||||
| chr2:101277221 | T | A | 1 | a0002c0002t0011 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*17A>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 7/7 | 17 | chr2 | 101277221 | ||||||
| chr2:101308664 | G | A | 1 | a0003c0003t0012 | 1 | HG02818.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-76C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/7 | chr2 | 101308664 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:101277399 | T | A | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1160-118A>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101277399 | |||||||
| chr2:101277504 | TC | T | 24 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0019 others(21): Show |
32 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1160-224delG | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101277504 | |||||||
| chr2:101277680 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0060 a0001c0001t0001g0087 others(1): Show |
5 | HG01261.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1160-399G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101277680 | |||||||
| chr2:101277760 | C | T | 44 | a0001c0001t0001g0064 a0002c0002t0001g0002 a0002c0002t0001g0003 others(41): Show |
103 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.1160-479G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101277760 | |||||||
| chr2:101277856 | C | CG | 9 | a0001c0001t0001g0028 a0001c0001t0001g0053 a0001c0001t0001g0076 others(6): Show |
10 | HG01175.hp1 HG01433.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.1160-576dupC | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101277856 | |||||||
| chr2:101278051 | C | CA | 20 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0014 others(17): Show |
51 | HG00609.hp2 HG00639.hp2 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.1160-771dupT | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101278051 | |||||||
| chr2:101278220 | C | T | 1 | a0002c0002t0001g0202 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1160-939G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101278220 | |||||||
| chr2:101278311 | C | G | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1160-1030G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101278311 | |||||||
| chr2:101278358 | A | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(182): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1160-1077T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101278358 | |||||||
| chr2:101278509 | A | G | 1 | a0002c0002t0001g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1160-1228T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101278509 | |||||||
| chr2:101278512 | TAA | T | 6 | a0002c0002t0001g0048 a0002c0002t0001g0147 a0002c0002t0001g0148 others(3): Show |
7 | HG01243.hp1 HG01358.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1160-1233_1160-123 others(6): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101278512 | |||||||
| chr2:101278568 | G | A | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1160-1287C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101278568 | |||||||
| chr2:101278575 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1160-1294A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101278575 | |||||||
| chr2:101278911 | G | A | 1 | a0002c0002t0001g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1160-1630C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101278911 | |||||||
| chr2:101278912 | A | C | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1160-1631T>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101278912 | |||||||
| chr2:101279072 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0059 a0001c0001t0003g0032 others(1): Show |
6 | HG00099.hp1 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.1160-1791C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101279072 | |||||||
| chr2:101279183 | C | T | 3 | a0001c0001t0001g0065 a0001c0001t0001g0075 a0001c0001t0001g0081 |
3 | NA18972.hp1 NA19083.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1160-1902G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101279183 | |||||||
| chr2:101279515 | T | C | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1160-2234A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101279515 | |||||||
| chr2:101279518 | G | A | 2 | a0002c0002t0001g0186 a0008c0010t0001g0220 |
2 | HG01496.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1160-2237C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101279518 | |||||||
| chr2:101279670 | C | T | 6 | a0002c0002t0001g0048 a0002c0002t0001g0147 a0002c0002t0001g0148 others(3): Show |
7 | HG01243.hp1 HG01358.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1159+2189G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101279670 | |||||||
| chr2:101280055 | G | A | 1 | a0003c0003t0004g0146 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1159+1804C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280055 | |||||||
| chr2:101280082 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1159+1777C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280082 | |||||||
| chr2:101280123 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1159+1736G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280123 | |||||||
| chr2:101280154 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1159+1705G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280154 | |||||||
| chr2:101280176 | A | AAATAATA others(14): Show |
1 | a0002c0002t0001g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1159+1662_1159+168 others(25): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280176 | |||||||
| chr2:101280201 | A | AATAATAA others(2): Show |
6 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(3): Show |
8 | HG00140.hp1 HG01175.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1159+1657_1159+165 others(13): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280201 | |||||||
| chr2:101280201 | A | AATAATG | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(74): Show |
128 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1159+1657_1159+165 others(10): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280201 | |||||||
| chr2:101280201 | A | AATGATG | 5 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0069 others(2): Show |
5 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1159+1652_1159+165 others(10): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280201 | |||||||
| chr2:101280201 | A | G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0035 others(3): Show |
8 | HG00140.hp2 HG00735.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.1159+1658T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280201 | |||||||
| chr2:101280204 | G | A | 1 | a0003c0003t0001g0151 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1159+1655C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280204 | |||||||
| chr2:101280402 | C | T | 1 | a0002c0002t0001g0014 | 4 | NA18960.hp2 NA18989.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1159+1457G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280402 | |||||||
| chr2:101280526 | A | G | 1 | a0002c0002t0001g0165 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1159+1333T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280526 | |||||||
| chr2:101280580 | C | T | 2 | a0003c0003t0001g0008 a0003c0003t0001g0145 |
6 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1159+1279G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280580 | |||||||
| chr2:101280833 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(74): Show |
133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1159+1026T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280833 | |||||||
| chr2:101280863 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(75): Show |
134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1159+996G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280863 | |||||||
| chr2:101280868 | C | T | 1 | a0002c0002t0001g0189 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1159+991G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280868 | |||||||
| chr2:101280869 | A | C | 1 | a0002c0002t0001g0189 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1159+990T>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280869 | |||||||
| chr2:101280880 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1159+979T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280880 | |||||||
| chr2:101280881 | A | G | 8 | a0002c0002t0001g0048 a0002c0002t0001g0147 a0002c0002t0001g0148 others(5): Show |
9 | HG01243.hp1 HG01358.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1159+978T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280881 | |||||||
| chr2:101280945 | G | A | 2 | a0003c0003t0001g0024 a0003c0003t0001g0039 |
5 | HG02809.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1159+914C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280945 | |||||||
| chr2:101280961 | G | A | 1 | a0002c0002t0001g0189 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1159+898C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280961 | |||||||
| chr2:101280962 | A | G | 1 | a0002c0002t0001g0189 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1159+897T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101280962 | |||||||
| chr2:101281090 | C | A | 1 | a0003c0003t0001g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1159+769G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281090 | |||||||
| chr2:101281131 | A | G | 1 | a0003c0003t0004g0146 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1159+728T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281131 | |||||||
| chr2:101281228 | CTG | C | 45 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0027 others(42): Show |
62 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.1159+629_1159+630d others(4): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281228 | |||||||
| chr2:101281343 | G | A | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1159+516C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281343 | |||||||
| chr2:101281401 | G | A | 1 | a0002c0002t0001g0192 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1159+458C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281401 | |||||||
| chr2:101281409 | C | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(182): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1159+450G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281409 | |||||||
| chr2:101281420 | A | ATTTTTTC others(3): Show |
1 | a0002c0002t0001g0189 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1159+429_1159+438d others(12): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281420 | |||||||
| chr2:101281489 | CT | C | 5 | a0001c0001t0001g0030 a0001c0001t0001g0059 a0001c0001t0001g0079 others(2): Show |
6 | HG02040.hp2 HG02965.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.1159+369delA | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281489 | |||||||
| chr2:101281511 | T | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(131): Show |
261 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1159+348A>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281511 | |||||||
| chr2:101281511 | T | TA | 52 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0027 others(49): Show |
70 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1159+347dupT | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281511 | |||||||
| chr2:101281625 | T | G | 1 | a0003c0003t0001g0151 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1159+234A>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281625 | |||||||
| chr2:101281683 | T | C | 1 | a0003c0003t0001g0177 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1159+176A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281683 | |||||||
| chr2:101281738 | C | T | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1159+121G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281738 | |||||||
| chr2:101281744 | G | A | 1 | a0002c0002t0001g0203 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1159+115C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281744 | |||||||
| chr2:101281760 | G | A | 45 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0027 others(42): Show |
62 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.1159+99C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281760 | |||||||
| chr2:101281775 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1159+84A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 6/6 | chr2 | 101281775 | |||||||
| chr2:101282079 | AAAAACAT others(11): Show |
A | 5 | a0003c0003t0004g0146 a0003c0003t0004g0179 a0003c0003t0004g0180 others(2): Show |
8 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-40_961-23delAA others(16): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282079 | |||||||
| chr2:101282161 | G | A | 1 | a0003c0003t0001g0049 | 2 | HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.961-104C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282161 | |||||||
| chr2:101282162 | T | C | 1 | a0003c0003t0001g0049 | 2 | HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.961-105A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282162 | |||||||
| chr2:101282207 | T | C | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.961-150A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282207 | |||||||
| chr2:101282562 | C | T | 2 | a0005c0005t0001g0092 a0005c0005t0001g0108 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.961-505G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282562 | |||||||
| chr2:101282668 | T | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(193): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.961-611A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282668 | |||||||
| chr2:101282941 | G | A | 1 | a0003c0003t0001g0024 | 3 | HG02809.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.961-884C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282941 | |||||||
| chr2:101282952 | T | A | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.961-895A>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282952 | |||||||
| chr2:101282969 | A | G | 45 | a0001c0001t0001g0064 a0002c0002t0001g0002 a0002c0002t0001g0003 others(42): Show |
104 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.961-912T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282969 | |||||||
| chr2:101282981 | C | G | 1 | a0002c0002t0001g0208 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.961-924G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282981 | |||||||
| chr2:101282984 | GC | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(83): Show |
143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.961-928delG | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101282984 | |||||||
| chr2:101283093 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.961-1036C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101283093 | |||||||
| chr2:101283218 | T | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0061 a0001c0001t0001g0085 |
11 | HG00438.hp1 HG00639.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.961-1161A>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101283218 | |||||||
| chr2:101283329 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.961-1272A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101283329 | |||||||
| chr2:101283391 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0059 |
3 | HG02040.hp2 NA18963.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.961-1334G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101283391 | |||||||
| chr2:101283417 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.961-1360G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101283417 | |||||||
| chr2:101283587 | G | A | 6 | a0002c0002t0001g0048 a0002c0002t0001g0147 a0002c0002t0001g0148 others(3): Show |
7 | HG01243.hp1 HG01358.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.961-1530C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101283587 | |||||||
| chr2:101283927 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0059 a0001c0001t0001g0078 |
4 | HG00280.hp2 HG02040.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.961-1870G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101283927 | |||||||
| chr2:101284038 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(197): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.961-1981A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284038 | |||||||
| chr2:101284078 | G | A | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.960+2003C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284078 | |||||||
| chr2:101284148 | T | C | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.960+1933A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284148 | |||||||
| chr2:101284205 | C | G | 1 | a0002c0002t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.960+1876G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284205 | |||||||
| chr2:101284276 | C | T | 1 | a0002c0002t0001g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.960+1805G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284276 | |||||||
| chr2:101284350 | C | T | 1 | a0002c0002t0001g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.960+1731G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284350 | |||||||
| chr2:101284373 | ATT | A | 2 | a0003c0003t0001g0008 a0003c0003t0001g0145 |
6 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.960+1706_960+1707d others(4): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284373 | |||||||
| chr2:101284535 | C | T | 1 | a0003c0003t0001g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.960+1546G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284535 | |||||||
| chr2:101284542 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(83): Show |
143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.960+1539A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284542 | |||||||
| chr2:101284552 | G | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0079 |
5 | NA18957.hp1 NA18973.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.960+1529C>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284552 | |||||||
| chr2:101284587 | C | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(83): Show |
143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.960+1494G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284587 | |||||||
| chr2:101284957 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.960+1124G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101284957 | |||||||
| chr2:101285014 | T | A | 1 | a0002c0002t0001g0216 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.960+1067A>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101285014 | |||||||
| chr2:101285051 | T | C | 2 | a0002c0002t0001g0206 a0002c0002t0009g0217 |
2 | HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.960+1030A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101285051 | |||||||
| chr2:101285150 | A | G | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.960+931T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101285150 | |||||||
| chr2:101285358 | G | A | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.960+723C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101285358 | |||||||
| chr2:101285411 | T | C | 5 | a0002c0002t0001g0025 a0002c0002t0001g0041 a0002c0002t0001g0043 others(2): Show |
9 | HG02080.hp1 NA18949.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.960+670A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101285411 | |||||||
| chr2:101285455 | T | C | 1 | a0001c0001t0001g0036 | 2 | HG01081.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.960+626A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101285455 | |||||||
| chr2:101285798 | C | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(182): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.960+283G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101285798 | |||||||
| chr2:101286065 | C | T | 1 | a0002c0002t0001g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.960+16G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 5/6 | chr2 | 101286065 | |||||||
| chr2:101286296 | A | G | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.864-119T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101286296 | |||||||
| chr2:101286409 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0059 a0001c0001t0001g0078 |
4 | HG00280.hp2 HG02040.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.864-232G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101286409 | |||||||
| chr2:101286823 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.864-646C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101286823 | |||||||
| chr2:101286854 | T | C | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.864-677A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101286854 | |||||||
| chr2:101286925 | T | C | 1 | a0003c0003t0001g0171 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.864-748A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101286925 | |||||||
| chr2:101287074 | C | T | 44 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0027 others(41): Show |
61 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.864-897G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101287074 | |||||||
| chr2:101287237 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.864-1060C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101287237 | |||||||
| chr2:101287286 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.864-1109C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101287286 | |||||||
| chr2:101287631 | A | T | 1 | a0001c0001t0001g0069 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.863+1342T>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101287631 | |||||||
| chr2:101287645 | C | T | 44 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0027 others(41): Show |
61 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.863+1328G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101287645 | |||||||
| chr2:101287743 | GA | G | 5 | a0002c0002t0001g0025 a0002c0002t0001g0041 a0002c0002t0001g0043 others(2): Show |
9 | HG02080.hp1 NA18949.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.863+1229delT | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101287743 | |||||||
| chr2:101287904 | A | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0077 |
2 | HG00099.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.863+1069T>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101287904 | |||||||
| chr2:101287944 | T | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(184): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.863+1029A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101287944 | |||||||
| chr2:101288058 | C | A | 1 | a0002c0002t0001g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.863+915G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288058 | |||||||
| chr2:101288058 | C | T | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.863+915G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288058 | |||||||
| chr2:101288230 | CT | C | 116 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0018 others(113): Show |
206 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.863+742delA | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288230 | |||||||
| chr2:101288230 | CTT | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(77): Show |
142 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.863+741_863+742del others(2): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288230 | |||||||
| chr2:101288260 | G | A | 1 | a0002c0002t0001g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.863+713C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288260 | |||||||
| chr2:101288387 | G | A | 1 | a0003c0003t0001g0151 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.863+586C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288387 | |||||||
| chr2:101288428 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.863+545C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288428 | |||||||
| chr2:101288446 | C | A | 1 | a0001c0001t0001g0086 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.863+527G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288446 | |||||||
| chr2:101288517 | C | A | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.863+456G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288517 | |||||||
| chr2:101288666 | A | C | 1 | a0001c0001t0001g0070 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.863+307T>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288666 | |||||||
| chr2:101288825 | T | C | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.863+148A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288825 | |||||||
| chr2:101288933 | C | G | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.863+40G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 4/6 | chr2 | 101288933 | |||||||
| chr2:101289084 | C | T | 1 | a0002c0002t0001g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.781-29G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289084 | |||||||
| chr2:101289100 | T | C | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.781-45A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289100 | |||||||
| chr2:101289143 | C | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0131 a0001c0001t0001g0132 |
4 | HG02074.hp2 HG02523.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.781-88G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289143 | |||||||
| chr2:101289233 | C | T | 5 | a0002c0002t0001g0025 a0002c0002t0001g0041 a0002c0002t0001g0043 others(2): Show |
9 | HG02080.hp1 NA18949.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.781-178G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289233 | |||||||
| chr2:101289429 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.781-374T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289429 | |||||||
| chr2:101289490 | G | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(182): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.781-435C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289490 | |||||||
| chr2:101289492 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.781-437C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289492 | |||||||
| chr2:101289560 | C | A | 1 | a0002c0002t0001g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.781-505G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289560 | |||||||
| chr2:101289610 | C | A | 1 | a0010c0009t0001g0219 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.781-555G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289610 | |||||||
| chr2:101289703 | G | A | 1 | a0002c0002t0001g0193 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.781-648C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289703 | |||||||
| chr2:101289707 | CA | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0068 others(3): Show |
6 | HG03492.hp1 NA18946.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.781-653delT | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289707 | |||||||
| chr2:101289708 | A | G | 1 | a0002c0002t0001g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.781-653T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289708 | |||||||
| chr2:101289773 | C | T | 1 | a0002c0002t0001g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.781-718G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101289773 | |||||||
| chr2:101290549 | A | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0125 |
2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.781-1494T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101290549 | |||||||
| chr2:101290603 | G | A | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.781-1548C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101290603 | |||||||
| chr2:101290840 | G | A | 1 | a0002c0002t0001g0048 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.781-1785C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101290840 | |||||||
| chr2:101290860 | T | G | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.781-1805A>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101290860 | |||||||
| chr2:101291213 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.781-2158G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101291213 | |||||||
| chr2:101291340 | G | A | 6 | a0003c0003t0001g0037 a0003c0003t0001g0040 a0003c0003t0001g0168 others(3): Show |
8 | HG01099.hp2 HG01255.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.781-2285C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101291340 | |||||||
| chr2:101291370 | C | T | 1 | a0002c0002t0001g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.781-2315G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101291370 | |||||||
| chr2:101291382 | C | CA | 4 | a0003c0003t0001g0038 a0003c0003t0001g0158 a0003c0003t0001g0159 others(1): Show |
5 | HG02622.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.781-2328_781-2327i others(3): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101291382 | |||||||
| chr2:101291400 | C | T | 1 | a0002c0002t0001g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.781-2345G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101291400 | |||||||
| chr2:101291450 | A | AT | 6 | a0001c0001t0001g0057 a0001c0001t0001g0069 a0002c0002t0001g0189 others(3): Show |
10 | HG00741.hp1 HG01255.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.781-2396dupA | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101291450 | |||||||
| chr2:101291564 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.780+2450G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101291564 | |||||||
| chr2:101291991 | G | A | 4 | a0001c0001t0001g0062 a0001c0001t0001g0066 a0001c0001t0001g0088 others(1): Show |
4 | NA18612.hp2 NA18999.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.780+2023C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101291991 | |||||||
| chr2:101292090 | T | C | 1 | a0009c0007t0001g0139 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.780+1924A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292090 | |||||||
| chr2:101292109 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.780+1905A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292109 | |||||||
| chr2:101292167 | T | C | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.780+1847A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292167 | |||||||
| chr2:101292181 | A | G | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.780+1833T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292181 | |||||||
| chr2:101292216 | T | C | 1 | a0003c0003t0001g0174 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.780+1798A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292216 | |||||||
| chr2:101292416 | T | TCAAAGAT others(211): Show |
1 | a0003c0003t0004g0180 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.780+1597_780+1598i others(220): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292416 | |||||||
| chr2:101292489 | G | A | 5 | a0002c0002t0001g0025 a0002c0002t0001g0041 a0002c0002t0001g0043 others(2): Show |
9 | HG02080.hp1 NA18949.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.780+1525C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292489 | |||||||
| chr2:101292526 | G | A | 1 | a0001c0001t0001g0022 | 3 | HG03710.hp2 NA18950.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.780+1488C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292526 | |||||||
| chr2:101292562 | G | C | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.780+1452C>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292562 | |||||||
| chr2:101292658 | C | T | 2 | a0001c0001t0001g0068 a0002c0002t0009g0217 |
2 | HG03225.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.780+1356G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292658 | |||||||
| chr2:101292683 | G | A | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.780+1331C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292683 | |||||||
| chr2:101292691 | G | A | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.780+1323C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292691 | |||||||
| chr2:101292840 | C | T | 5 | a0002c0002t0001g0025 a0002c0002t0001g0041 a0002c0002t0001g0043 others(2): Show |
9 | HG02080.hp1 NA18949.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.780+1174G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292840 | |||||||
| chr2:101292897 | A | C | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.780+1117T>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292897 | |||||||
| chr2:101292972 | CT | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(76): Show |
133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.780+1041delA | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101292972 | |||||||
| chr2:101293093 | C | T | 1 | a0003c0003t0001g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.780+921G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101293093 | |||||||
| chr2:101293190 | C | A | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.780+824G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101293190 | |||||||
| chr2:101293594 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.780+420A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101293594 | |||||||
| chr2:101293664 | T | C | 3 | a0003c0003t0001g0008 a0003c0003t0001g0145 a0003c0003t0001g0199 |
7 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.780+350A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101293664 | |||||||
| chr2:101293773 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.780+241G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101293773 | |||||||
| chr2:101293908 | C | T | 1 | a0002c0002t0001g0207 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.780+106G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101293908 | |||||||
| chr2:101293962 | C | T | 1 | a0002c0002t0001g0188 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.780+52G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101293962 | |||||||
| chr2:101293992 | A | G | 1 | a0002c0002t0001g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.780+22T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 3/6 | chr2 | 101293992 | |||||||
| chr2:101294113 | G | A | 1 | a0003c0003t0001g0169 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.712-31C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294113 | |||||||
| chr2:101294217 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.712-135A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294217 | |||||||
| chr2:101294244 | C | A | 2 | a0003c0003t0001g0024 a0003c0003t0001g0039 |
5 | HG02809.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.712-162G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294244 | |||||||
| chr2:101294344 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0115 |
2 | HG02738.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.712-262G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294344 | |||||||
| chr2:101294466 | G | A | 1 | a0003c0003t0001g0151 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.712-384C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294466 | |||||||
| chr2:101294533 | C | T | 1 | a0004c0004t0002g0016 | 4 | HG02258.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+398G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294533 | |||||||
| chr2:101294573 | C | T | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.711+358G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294573 | |||||||
| chr2:101294674 | C | G | 1 | a0002c0002t0001g0187 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.711+257G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294674 | |||||||
| chr2:101294676 | G | C | 1 | a0002c0002t0001g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.711+255C>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294676 | |||||||
| chr2:101294794 | C | A | 1 | a0001c0001t0001g0097 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.711+137G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294794 | |||||||
| chr2:101294830 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0091 |
4 | HG00280.hp1 HG00738.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+101C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294830 | |||||||
| chr2:101294879 | A | G | 5 | a0003c0003t0004g0146 a0003c0003t0004g0179 a0003c0003t0004g0180 others(2): Show |
8 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.711+52T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294879 | |||||||
| chr2:101294923 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(83): Show |
143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
splice_region_variant&intron_variant | LOW | c.711+8T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 2/6 | chr2 | 101294923 | |||||||
| chr2:101295189 | A | G | 2 | a0002c0002t0001g0186 a0008c0010t0001g0220 |
2 | HG01496.hp2 HG02602.hp1 |
splice_region_variant&intron_variant | LOW | c.461-8T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295189 | |||||||
| chr2:101295230 | C | A | 7 | a0003c0003t0001g0024 a0003c0003t0001g0038 a0003c0003t0001g0039 others(4): Show |
11 | HG02572.hp1 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.461-49G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295230 | |||||||
| chr2:101295381 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.461-200G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295381 | |||||||
| chr2:101295436 | C | T | 2 | a0003c0003t0001g0008 a0003c0003t0001g0145 |
6 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.461-255G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295436 | |||||||
| chr2:101295552 | T | C | 1 | a0003c0003t0001g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.461-371A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295552 | |||||||
| chr2:101295607 | G | A | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-426C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295607 | |||||||
| chr2:101295615 | C | A | 1 | a0001c0001t0001g0109 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.461-434G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295615 | |||||||
| chr2:101295615 | C | T | 5 | a0002c0002t0001g0025 a0002c0002t0001g0041 a0002c0002t0001g0043 others(2): Show |
9 | HG02080.hp1 NA18949.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.461-434G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295615 | |||||||
| chr2:101295636 | G | A | 1 | a0002c0002t0001g0042 | 2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.461-455C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295636 | |||||||
| chr2:101295639 | C | A | 5 | a0002c0002t0001g0025 a0002c0002t0001g0041 a0002c0002t0001g0043 others(2): Show |
9 | HG02080.hp1 NA18949.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.461-458G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295639 | |||||||
| chr2:101295658 | C | A | 41 | a0002c0002t0001g0025 a0002c0002t0001g0041 a0002c0002t0001g0042 others(38): Show |
62 | HG00642.hp2 HG01074.hp2 HG01099.hp2 others(59): Show |
intron_variant | MODIFIER | c.461-477G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295658 | |||||||
| chr2:101295660 | C | CA | 6 | a0001c0001t0001g0093 a0001c0001t0001g0143 a0003c0003t0001g0159 others(3): Show |
6 | HG01361.hp2 HG02622.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.461-480dupT | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295660 | |||||||
| chr2:101295670 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.461-489T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295670 | |||||||
| chr2:101295969 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0124 a0001c0001t0006g0123 |
4 | HG02015.hp1 HG02602.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.461-788G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101295969 | |||||||
| chr2:101296096 | C | T | 1 | a0002c0002t0001g0154 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.461-915G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101296096 | |||||||
| chr2:101296120 | T | C | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-939A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101296120 | |||||||
| chr2:101296278 | A | T | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-1097T>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101296278 | |||||||
| chr2:101296657 | G | T | 5 | a0001c0001t0001g0064 a0002c0002t0001g0045 a0002c0002t0001g0162 others(2): Show |
6 | HG00438.hp2 HG00544.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.461-1476C>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101296657 | |||||||
| chr2:101296659 | C | T | 2 | a0001c0001t0001g0102 a0001c0001t0001g0142 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.461-1478G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101296659 | |||||||
| chr2:101296850 | A | T | 3 | a0003c0003t0001g0167 a0003c0003t0001g0170 a0003c0003t0001g0171 |
3 | HG01167.hp2 HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.461-1669T>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101296850 | |||||||
| chr2:101296859 | T | A | 12 | a0002c0002t0001g0216 a0003c0003t0001g0023 a0003c0003t0001g0049 others(9): Show |
15 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.461-1678A>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101296859 | |||||||
| chr2:101297037 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.461-1856G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297037 | |||||||
| chr2:101297081 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.461-1900G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297081 | |||||||
| chr2:101297122 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.461-1941A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297122 | |||||||
| chr2:101297288 | A | G | 1 | a0002c0002t0001g0042 | 2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.461-2107T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297288 | |||||||
| chr2:101297291 | A | T | 3 | a0002c0002t0001g0005 a0002c0002t0001g0201 a0002c0002t0011g0200 |
10 | HG01884.hp1 HG02486.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.461-2110T>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297291 | |||||||
| chr2:101297488 | C | T | 6 | a0002c0002t0001g0048 a0002c0002t0001g0147 a0002c0002t0001g0148 others(3): Show |
7 | HG01243.hp1 HG01358.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.461-2307G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297488 | |||||||
| chr2:101297547 | T | TG | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(83): Show |
143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.461-2367dupC | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297547 | |||||||
| chr2:101297592 | C | G | 1 | a0001c0001t0001g0066 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.461-2411G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297592 | |||||||
| chr2:101297758 | A | G | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-2577T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297758 | |||||||
| chr2:101297821 | G | T | 1 | a0003c0003t0001g0157 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.461-2640C>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297821 | |||||||
| chr2:101297825 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.461-2644G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297825 | |||||||
| chr2:101297846 | C | T | 3 | a0002c0002t0001g0005 a0002c0002t0001g0201 a0002c0002t0011g0200 |
10 | HG01884.hp1 HG02486.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.461-2665G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297846 | |||||||
| chr2:101297951 | T | C | 21 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0014 others(18): Show |
52 | HG00609.hp2 HG00639.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.461-2770A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297951 | |||||||
| chr2:101297969 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0115 |
2 | HG02738.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.461-2788G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297969 | |||||||
| chr2:101297984 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.461-2803C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101297984 | |||||||
| chr2:101298016 | T | G | 3 | a0003c0003t0001g0168 a0003c0003t0001g0176 a0003c0003t0001g0177 |
3 | HG01099.hp2 HG01255.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.461-2835A>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101298016 | |||||||
| chr2:101298312 | C | G | 1 | a0002c0002t0001g0181 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.461-3131G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101298312 | |||||||
| chr2:101298373 | T | A | 1 | a0003c0003t0012g0221 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.461-3192A>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101298373 | |||||||
| chr2:101298509 | G | A | 1 | a0005c0005t0001g0094 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.461-3328C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101298509 | |||||||
| chr2:101298516 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG02040.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.461-3335C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101298516 | |||||||
| chr2:101298560 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0142 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.461-3379C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101298560 | |||||||
| chr2:101298685 | G | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG00673.hp1 HG02135.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.461-3504C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101298685 | |||||||
| chr2:101298701 | A | G | 1 | a0008c0010t0001g0220 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.461-3520T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101298701 | |||||||
| chr2:101298852 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.461-3671G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101298852 | |||||||
| chr2:101298947 | T | C | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-3766A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101298947 | |||||||
| chr2:101299047 | C | T | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-3866G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299047 | |||||||
| chr2:101299075 | C | T | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-3894G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299075 | |||||||
| chr2:101299086 | T | C | 1 | a0002c0002t0001g0209 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.461-3905A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299086 | |||||||
| chr2:101299094 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.461-3913A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299094 | |||||||
| chr2:101299142 | C | T | 1 | a0002c0002t0001g0044 | 2 | HG01069.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.461-3961G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299142 | |||||||
| chr2:101299161 | C | T | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-3980G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299161 | |||||||
| chr2:101299187 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.461-4006A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299187 | |||||||
| chr2:101299288 | T | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0110 |
4 | HG02896.hp2 HG03041.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.461-4107A>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299288 | |||||||
| chr2:101299442 | C | T | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-4261G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299442 | |||||||
| chr2:101299580 | GC | G | 1 | a0002c0002t0001g0015 | 4 | HG02622.hp2 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.461-4400delG | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299580 | |||||||
| chr2:101299582 | T | A | 1 | a0002c0002t0001g0015 | 4 | HG02622.hp2 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.461-4401A>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299582 | |||||||
| chr2:101299633 | G | C | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-4452C>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299633 | |||||||
| chr2:101299645 | C | T | 1 | a0002c0002t0001g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.461-4464G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299645 | |||||||
| chr2:101299765 | T | C | 25 | a0002c0002t0001g0216 a0003c0003t0001g0023 a0003c0003t0001g0024 others(22): Show |
34 | HG00642.hp2 HG01074.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.461-4584A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299765 | |||||||
| chr2:101299834 | T | C | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-4653A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299834 | |||||||
| chr2:101299915 | G | A | 1 | a0002c0002t0001g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.461-4734C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101299915 | |||||||
| chr2:101300206 | G | A | 1 | a0002c0002t0001g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.461-5025C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300206 | |||||||
| chr2:101300297 | G | A | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-5116C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300297 | |||||||
| chr2:101300326 | C | G | 5 | a0002c0002t0001g0025 a0002c0002t0001g0041 a0002c0002t0001g0043 others(2): Show |
9 | HG02080.hp1 NA18949.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.461-5145G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300326 | |||||||
| chr2:101300371 | T | C | 5 | a0002c0002t0001g0025 a0002c0002t0001g0041 a0002c0002t0001g0043 others(2): Show |
9 | HG02080.hp1 NA18949.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.461-5190A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300371 | |||||||
| chr2:101300402 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.461-5221G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300402 | |||||||
| chr2:101300427 | A | G | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-5246T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300427 | |||||||
| chr2:101300620 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(77): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.461-5439G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300620 | |||||||
| chr2:101300725 | G | A | 1 | a0002c0002t0001g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.461-5544C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300725 | |||||||
| chr2:101300864 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.461-5683A>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300864 | |||||||
| chr2:101300881 | G | A | 1 | a0002c0002t0001g0042 | 2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.461-5700C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300881 | |||||||
| chr2:101300903 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(127): Show |
209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.461-5722G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300903 | |||||||
| chr2:101300997 | T | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(78): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.461-5816A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101300997 | |||||||
| chr2:101301049 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(78): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.461-5868C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101301049 | |||||||
| chr2:101301238 | G | GT | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(75): Show |
133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.461-6058dupA | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101301238 | |||||||
| chr2:101301331 | A | AT | 5 | a0001c0001t0001g0065 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
6 | HG02559.hp2 HG03130.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.461-6151dupA | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101301331 | |||||||
| chr2:101301331 | AT | A | 6 | a0002c0002t0001g0206 a0003c0003t0004g0146 a0003c0003t0004g0179 others(3): Show |
9 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.461-6151delA | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101301331 | |||||||
| chr2:101301689 | TTTTG | T | 29 | a0002c0002t0001g0216 a0003c0003t0001g0008 a0003c0003t0001g0023 others(26): Show |
42 | HG00642.hp2 HG01074.hp2 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.460+6436_460+6439d others(6): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101301689 | |||||||
| chr2:101301770 | T | A | 1 | a0001c0001t0001g0101 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.460+6359A>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101301770 | |||||||
| chr2:101301771 | C | A | 1 | a0001c0001t0001g0138 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.460+6358G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101301771 | |||||||
| chr2:101301771 | C | G | 4 | a0003c0003t0001g0038 a0003c0003t0001g0158 a0003c0003t0001g0159 others(1): Show |
5 | HG02622.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.460+6358G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101301771 | |||||||
| chr2:101301779 | G | C | 1 | a0001c0001t0001g0129 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.460+6350C>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101301779 | |||||||
| chr2:101301823 | C | T | 1 | a0002c0002t0011g0200 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.460+6306G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101301823 | |||||||
| chr2:101302033 | T | C | 1 | a0002c0002t0001g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.460+6096A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302033 | |||||||
| chr2:101302116 | C | T | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460+6013G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302116 | |||||||
| chr2:101302196 | T | C | 1 | a0002c0002t0001g0204 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.460+5933A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302196 | |||||||
| chr2:101302245 | G | T | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460+5884C>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302245 | |||||||
| chr2:101302262 | A | G | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460+5867T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302262 | |||||||
| chr2:101302340 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(78): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.460+5789T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302340 | |||||||
| chr2:101302445 | G | A | 4 | a0001c0001t0001g0102 a0001c0001t0001g0142 a0002c0002t0001g0153 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.460+5684C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302445 | |||||||
| chr2:101302489 | T | C | 1 | a0002c0002t0001g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.460+5640A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302489 | |||||||
| chr2:101302586 | T | C | 1 | a0002c0002t0001g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460+5543A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302586 | |||||||
| chr2:101302630 | T | C | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460+5499A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302630 | |||||||
| chr2:101302697 | C | T | 1 | a0002c0002t0001g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.460+5432G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302697 | |||||||
| chr2:101302912 | C | A | 5 | a0001c0001t0001g0034 a0001c0001t0001g0130 a0001c0001t0001g0131 others(2): Show |
6 | HG02074.hp2 HG02080.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.460+5217G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302912 | |||||||
| chr2:101302941 | T | C | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460+5188A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302941 | |||||||
| chr2:101302981 | TA | T | 43 | a0001c0001t0001g0064 a0001c0001t0001g0118 a0002c0002t0001g0002 others(40): Show |
105 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.460+5147delT | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302981 | |||||||
| chr2:101302981 | TAA | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(123): Show |
205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.460+5146_460+5147d others(4): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101302981 | |||||||
| chr2:101303077 | G | C | 37 | a0002c0002t0001g0048 a0002c0002t0001g0147 a0002c0002t0001g0148 others(34): Show |
51 | HG00642.hp2 HG01074.hp2 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.460+5052C>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303077 | |||||||
| chr2:101303261 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG00140.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.460+4868T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303261 | |||||||
| chr2:101303274 | T | C | 2 | a0002c0002t0001g0206 a0002c0002t0009g0217 |
2 | HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.460+4855A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303274 | |||||||
| chr2:101303281 | AT | A | 133 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0033 others(130): Show |
230 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(227): Show |
intron_variant | MODIFIER | c.460+4847delA | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303281 | |||||||
| chr2:101303281 | ATT | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(78): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.460+4846_460+4847d others(4): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303281 | |||||||
| chr2:101303373 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.460+4756G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303373 | |||||||
| chr2:101303430 | A | C | 1 | a0001c0001t0001g0114 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.460+4699T>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303430 | |||||||
| chr2:101303602 | T | A | 1 | a0003c0003t0001g0145 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.460+4527A>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303602 | |||||||
| chr2:101303643 | C | T | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460+4486G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303643 | |||||||
| chr2:101303643 | CATACCTC others(80): Show |
C | 1 | a0002c0002t0001g0198 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.460+4399_460+4485d others(89): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303643 | |||||||
| chr2:101303708 | C | A | 1 | a0001c0001t0001g0022 | 3 | HG03710.hp2 NA18950.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.460+4421G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303708 | |||||||
| chr2:101303710 | TATCAATA others(80): Show |
T | 1 | a0002c0002t0001g0178 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.460+4332_460+4418d others(89): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303710 | |||||||
| chr2:101303815 | C | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG03834.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.460+4314G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303815 | |||||||
| chr2:101303817 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(77): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.460+4312A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303817 | |||||||
| chr2:101303829 | T | C | 29 | a0002c0002t0001g0216 a0003c0003t0001g0008 a0003c0003t0001g0023 others(26): Show |
42 | HG00642.hp2 HG01074.hp2 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.460+4300A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303829 | |||||||
| chr2:101303895 | C | A | 3 | a0002c0002t0001g0005 a0002c0002t0001g0201 a0002c0002t0011g0200 |
10 | HG01884.hp1 HG02486.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.460+4234G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303895 | |||||||
| chr2:101303906 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.460+4223A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101303906 | |||||||
| chr2:101304175 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.460+3954A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304175 | |||||||
| chr2:101304265 | C | G | 7 | a0003c0003t0001g0024 a0003c0003t0001g0038 a0003c0003t0001g0039 others(4): Show |
11 | HG02572.hp1 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.460+3864G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304265 | |||||||
| chr2:101304393 | C | T | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460+3736G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304393 | |||||||
| chr2:101304511 | C | T | 1 | a0001c0001t0007g0063 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.460+3618G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304511 | |||||||
| chr2:101304622 | T | C | 1 | a0002c0002t0001g0202 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.460+3507A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304622 | |||||||
| chr2:101304630 | A | T | 1 | a0002c0002t0001g0041 | 2 | NA19058.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.460+3499T>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304630 | |||||||
| chr2:101304835 | A | AT | 8 | a0001c0001t0001g0051 a0001c0001t0001g0112 a0001c0001t0001g0113 others(5): Show |
11 | HG00642.hp2 HG01074.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.460+3293dupA | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304835 | |||||||
| chr2:101304835 | AT | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(124): Show |
256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.460+3293delA | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304835 | |||||||
| chr2:101304835 | ATT | A | 6 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(3): Show |
6 | HG01167.hp1 HG01257.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.460+3292_460+3293d others(4): Show |
RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304835 | |||||||
| chr2:101304897 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.460+3232C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304897 | |||||||
| chr2:101304966 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.460+3163C>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101304966 | |||||||
| chr2:101305098 | T | C | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460+3031A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101305098 | |||||||
| chr2:101305290 | C | A | 1 | a0001c0001t0001g0035 | 2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.460+2839G>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101305290 | |||||||
| chr2:101305341 | C | G | 1 | a0002c0002t0001g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.460+2788G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101305341 | |||||||
| chr2:101305701 | G | A | 2 | a0002c0002t0001g0015 a0002c0002t0001g0206 |
5 | HG02622.hp2 HG02922.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.460+2428C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101305701 | |||||||
| chr2:101305708 | T | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(179): Show |
326 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(323): Show |
intron_variant | MODIFIER | c.460+2421A>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101305708 | |||||||
| chr2:101305722 | G | A | 1 | a0002c0002t0001g0205 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.460+2407C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101305722 | |||||||
| chr2:101305725 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(169): Show |
315 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.460+2404C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101305725 | |||||||
| chr2:101305792 | G | A | 2 | a0002c0002t0001g0015 a0002c0002t0001g0206 |
5 | HG02622.hp2 HG02922.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.460+2337C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101305792 | |||||||
| chr2:101305850 | G | A | 7 | a0002c0002t0001g0006 a0002c0002t0001g0047 a0002c0002t0001g0207 others(4): Show |
14 | NA18939.hp1 NA18950.hp1 NA18956.hp1 others(11): Show |
intron_variant | MODIFIER | c.460+2279C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101305850 | |||||||
| chr2:101305898 | A | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(77): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.460+2231T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101305898 | |||||||
| chr2:101306024 | G | A | 6 | a0002c0002t0001g0048 a0002c0002t0001g0147 a0002c0002t0001g0148 others(3): Show |
7 | HG01243.hp1 HG01358.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.460+2105C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306024 | |||||||
| chr2:101306031 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.460+2098C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306031 | |||||||
| chr2:101306117 | G | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG00621.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.460+2012C>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306117 | |||||||
| chr2:101306234 | C | G | 1 | a0002c0002t0001g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.460+1895G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306234 | |||||||
| chr2:101306264 | C | T | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460+1865G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306264 | |||||||
| chr2:101306265 | G | A | 2 | a0002c0002t0009g0217 a0003c0003t0001g0215 |
2 | HG03017.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.460+1864C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306265 | |||||||
| chr2:101306311 | T | C | 101 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(98): Show |
188 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(185): Show |
intron_variant | MODIFIER | c.460+1818A>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306311 | |||||||
| chr2:101306418 | G | A | 2 | a0002c0002t0001g0216 a0003c0003t0001g0049 |
3 | HG02698.hp2 HG03654.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.460+1711C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306418 | |||||||
| chr2:101306461 | G | A | 1 | a0002c0002t0009g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460+1668C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306461 | |||||||
| chr2:101306535 | C | G | 1 | a0001c0001t0001g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.460+1594G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306535 | |||||||
| chr2:101306833 | C | T | 1 | a0003c0003t0001g0151 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.460+1296G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306833 | |||||||
| chr2:101306840 | T | G | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.460+1289A>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306840 | |||||||
| chr2:101306874 | C | T | 3 | a0002c0002t0001g0012 a0002c0002t0001g0149 a0002c0002t0001g0150 |
6 | HG01123.hp2 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.460+1255G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101306874 | |||||||
| chr2:101307024 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.460+1105C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101307024 | |||||||
| chr2:101307234 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG01081.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.460+895C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101307234 | |||||||
| chr2:101307356 | A | C | 2 | a0002c0002t0001g0147 a0002c0002t0001g0148 |
2 | HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.460+773T>G | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101307356 | |||||||
| chr2:101307542 | A | G | 104 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(101): Show |
191 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(188): Show |
intron_variant | MODIFIER | c.460+587T>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101307542 | |||||||
| chr2:101307574 | C | T | 1 | a0003c0003t0004g0146 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.460+555G>A | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101307574 | |||||||
| chr2:101307913 | C | G | 2 | a0003c0003t0001g0008 a0003c0003t0001g0145 |
6 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.460+216G>C | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101307913 | |||||||
| chr2:101307914 | G | A | 1 | a0002c0002t0001g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.460+215C>T | RNF149 | ENSG00000163162.9 | transcript | ENST00000295317.4 | protein_coding | 1/6 | chr2 | 101307914 |